16 Therapeutic Areas Jobs

As an Expert Scientific Writer at Novartis Healthcare Private Limited in Hyderabad, your primary responsibility will be to manage and complete various Medical Communications deliverables with high quality standards and within agreed timelines. Your projects will include manuscripts, abstracts, posters, slide sets, satellite symposia content, congress or advisory board reports, publication planning, and medical education materials for internal medical and/or clinical teams. Key Responsibilities: - Demonstrate a command of assigned therapeutic areas and expertise with assigned products - Research and write original content for various publications activities - Prepare meeting materials for sat...

As a Consultant in Primary Market Research at PharmaACE, a growing Global Healthcare Consulting Firm based in Princeton, New Jersey, you will play a vital role in designing and executing high-quality primary research for leading global pharmaceutical clients. Your responsibilities will include market research design, data analysis, client management, project management, industry expertise, and innovation. Key Responsibilities: - Develop and implement primary market research strategies tailored to address specific business objectives of clients. - Design qualitative and quantitative research studies such as surveys and in-depth interviews. - Analyze primary data to identify trends, behaviors,...

You will be responsible for performing comprehensive Quality Control (QC) review of clinical sections of regulatory documents to ensure the highest quality from technical, regulatory, and compliance perspectives. This includes verifying all references and source data, ensuring internal consistency within documents, and documenting QC findings appropriately. Additionally, you will be involved in content QC of clinical data/reports across different therapeutic areas, development phases, modalities, and geographic regions. - Conduct comprehensive QC review of clinical sections in regulatory documents such as IBs, INDs, NDAs, BLAs, CTAs, MAAs, and briefing packages for regulatory agency meetings...

As a Medico Marketing professional at Intas Pharmaceuticals, your role will involve handling the medico marketing responsibilities of the assigned business unit/s. Your primary objective will be to provide internal medical and scientific support to the designated therapeutic areas. You will contribute to product/therapy strategy, engage with key customers including national Key Opinion Leaders (KOLs), and facilitate various scientific initiatives like advisory board meetings, scientific symposia, and medical education sessions. Key Responsibilities: - Serve as an internal medical and scientific resource for assigned therapeutic areas - Assist in devising Product/Therapy Strategy - Provide me...

Role Overview: As a Medical Advisor at Intas Pharmaceuticals, you will be responsible for handling the medico marketing responsibilities of the assigned business unit/s. Your role will involve strategic support, customer engagement, and training and development in the medical and scientific aspect of the business. Key Responsibilities: - Strategic Support: - Serve as an internal medical and scientific resource to assigned therapeutic areas - Support in devising Product/Therapy Strategy - Provide medical/clinical oversight regarding positioning strategy and implementation tactics for respective products - Stay updated on new developments, publications, and trends in different therapy areas - ...

As a member of the Advisory Acceleration Centre at PwC, you will be part of a team that provides premium, cost-effective, high-quality services to support process quality and delivery capability for client engagements. Your role will involve working with global clients in the Management Consulting team to design and implement growth, operational, and customer-focused strategies for sustainable competitive advantage. Your thought leadership and experience will help clients navigate challenges and turn them into market advantages across the value chain and around the globe. Key Responsibilities: - Work with client and project teams to support global engagements by conducting analyses, developi...

Role Overview: As a Senior Clinical Programmer at Syneos Health, you will play a crucial role in accelerating customer success by translating clinical, medical affairs, and commercial insights into outcomes. You will be part of a team that puts the customer and patient at the center of everything they do, aiming to simplify and streamline work processes for enhanced collaboration and innovation. Your contributions will be pivotal in helping customers achieve their goals and ultimately changing lives. Key Responsibilities: - Utilize primary development tools such as Medidata, Rave, Oracle OC/RDC, Oracle Inform, and SAS to design, write, validate, and maintain software in adherence to specific...

Role Overview: As a Medical Affairs Manager, you will play a crucial role in bridging the gap between the company and the healthcare community. Your responsibilities will include driving evidence-based communication, stakeholder engagement, and supporting various medical initiatives. You will lead scientific discussions, manage Key Opinion Leader (KOL) engagements, and contribute to the development and execution of medical strategies. Key Responsibilities: - Provide regular scientific updates and ensure the accuracy of all scientific content shared with the marketing team. - Review, approve, and guide all scientific communications for both internal and external use. - Generate and evaluate i...

Role Overview: You will be responsible for providing medical expertise and support to the Sales Force for Pharma, vaccines, and Nutrition. This includes offering expert medical and scientific input to both internal and external stakeholders, staying updated on the latest scientific literature and clinical developments, responding to medical inquiries from healthcare professionals, patients, and internal teams, as well as developing and maintaining medical information resources. Key Responsibilities: - Identify, develop, and maintain relationships with Key Opinion Leaders (KOLs). - Organize and participate in advisory boards, speaker programs, and other medical education activities. - Gather ...

As the Medical Scientific Expert for the assigned product(s) and relevant therapeutic areas, your role will involve being the key medical scientific voice of expertise. You will provide expert advice and guidance to Healthcare Professionals (HCPs) and facilitate information, education, and research activities. Your responsibilities include: - Acting as the medical scientific expert for assigned products and therapeutic areas - Providing advice, guidance, and information to HCPs - Facilitating scientific exchange and developing professional relationships with key opinion leaders - Contributing medical scientific input into marketing strategy and commercial initiatives - Maintaining in-depth k...

The Expert Scientific Writer role at Novartis in Hyderabad involves managing and completing assigned Medical Communications deliverables with high quality standards and adherence to agreed timelines. This includes working on projects such as manuscripts, abstracts, posters, slide sets, satellite symposia content, congress or advisory board reports, publication planning, and medical education materials for internal medical and/or clinical teams. Key responsibilities of this role include demonstrating expertise in assigned therapeutic areas and products, researching and writing original content for various publication activities, preparing meeting materials for satellite symposia and reports f...

As a Medical Advisor at our company, you will play a crucial role in supporting medical affairs through your scientific and clinical expertise. Your responsibilities will include providing scientific and clinical input to various teams, responding to medical queries, conducting literature reviews, developing training materials, engaging with Key Opinion Leaders, ensuring compliance with guidelines, and maintaining accurate records. You will be expected to collaborate effectively with cross-functional teams such as marketing, sales, and regulatory, ensuring the accuracy and compliance of promotional materials. Additionally, you will be responsible for responding to medical queries from intern...

As a Lead Medical Writer, you will be responsible for developing and reviewing medical writing deliverables that support the clinical regulatory writing portfolio. Your role will also involve training junior writers. You must have 4 to 6 years of experience in writing Clinical & Regulatory documents supporting global filings, specifically with experience in CTD Module 2 and Module 5. Your responsibilities will include preparing/reviewing clinical study reports, protocols, investigator brochures, submission data summaries, and other regulatory documents on investigational drugs at various stages of clinical development. You will apply lean authoring principles and coordinate activities for do...

As a Clinical Research Medical Advisor (CRMA) at Novartis, located in Mumbai, you will play a crucial role in overseeing all clinical and medical aspects related to Development and prioritized Research programs/trials in the country. Your responsibilities will include providing clinical strategic and tactical leadership, ensuring optimal clinical trial implementation, and upholding safety standards and clinical data quality. Your key responsibilities will involve offering clinical development and indication expertise specific to the country/cluster, validating study designs, contributing to scientific/clinical/medical aspects during the start-up phase, providing clinical/medical expertise to...

As the Medical Scientific Expert for the assigned product(s) and relevant therapeutic areas, your role will involve providing expert advice and guidance to healthcare professionals. You will play a key role in facilitating information, education, and research activities for physicians and ancillary healthcare professionals, focusing on current and future therapies in development or already commercialized. Your responsibilities will include engaging in scientific exchange and developing professional relationships with key opinion leaders. Additionally, you will be expected to provide medical scientific input into marketing strategies and key commercial initiatives. To excel in this role, you ...

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